Zobrazeno 1 - 10
of 180
pro vyhledávání: '"C. Delescluse"'
Publikováno v:
Annales Pharmaceutiques Françaises. 72:112-121
Resume Introduction L’objectif de ce travail etait de diminuer les risques d’erreurs lors de l’administration par voie orale de medicaments au nourrisson (âge de 28 jours a 2 ans). Materiel et methode La methode de l’analyse preliminaire des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60d7fbe9b0ecd555a3694623651bb1c0
https://doi.org/10.1016/j.pharma.2013.11.002
https://doi.org/10.1016/j.pharma.2013.11.002
Autor:
C. Delescluse, Thierry H. Pham
Publikováno v:
L'Encéphale. 31:683-691
Resume L’etude evalue la prevalence du trouble de la personnalite sadique (TPS, DSM III-R) et ses relations avec les criteres de la psychopathie selon la PCL-R (Hare, 1991) en milieu psychiatrique securitaire. Le TPS est defini a partir de 8 items
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfb8cbd44b048e5c3456b2be566c80b1
https://doi.org/10.1016/s0013-7006(05)82426-1
https://doi.org/10.1016/s0013-7006(05)82426-1
Autor:
Roger Rahmani, Pierre Lesca, Madeleine Pralavorio, Géraldine Lemaire, N. Ledirac, C. Delescluse
Publikováno v:
Life Sciences
Life Sciences, Elsevier, 2004, 74, pp.2265-2278
Life Sciences, Elsevier, 2004, 74, pp.2265-2278
Benzimidazoles compounds like omeprazole (OME) and thiabendazole (TBZ) mediate CYP1A1 induction differently from classical aryl hydrocarbon receptor (AhR) ligands, 3-methylcholanthrene (3-MC) and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). To clarify
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdb2fff108ec0d3683fa4a314a16d812
https://doi.org/10.1016/j.lfs.2003.09.056
https://doi.org/10.1016/j.lfs.2003.09.056
Autor:
Marie P. Piechocki, Xavier Gidrol, C. Delescluse, Roger Rahmani, N. Ledirac, Ronald N. Hines, Rouya Li
Publikováno v:
Biochemical Pharmacology. 61:399-407
Carbaryl and thiabendazole, two widely used pesticides, have been shown to induce cytochrome P450 1A1 (CYP1A1) expression, but neither compound is capable of displacing [3H] 2,3,7,8-tetrachlorodibenzo-P-dioxin from its aryl hydrocarbon receptor bindi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5136ab4ec772e83db632aa726705c33
https://doi.org/10.1016/s0006-2952(00)00562-1
https://doi.org/10.1016/s0006-2952(00)00562-1
Autor:
Pierre Lesca, G. de Sousa, Madeleine Pralavorio, C. Delescluse, Ronald N. Hines, Marie P. Piechocki, Roger Rahmani, N. Ledirac
Publikováno v:
Toxicology and Applied Pharmacology. 164:273-279
Diflubenzuron (DFB) belongs to a group of compounds called benzoyphenyl ureas acting as chitin synthesis inhibitors, which also inhibit growth of B16 murine melanomas. The present study was designed to investigate the effect of this insecticide, on C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5fd4484abeae25126aadd50e40bdc0f
https://doi.org/10.1006/taap.2000.8920
https://doi.org/10.1006/taap.2000.8920
Publikováno v:
Biochemical Pharmacology. 57:255-262
Malaria remains the most prevalent infectious disease of tropical and subtropical areas of the world. It represents a crucial problem in public health care, affecting 750 million people annually, of whom at least two million die. Various antimalarial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0d6509df654180501692d706f98b13a
https://doi.org/10.1016/s0006-2952(98)00304-9
https://doi.org/10.1016/s0006-2952(98)00304-9
Publikováno v:
Annales pharmaceutiques francaises. 72(2)
The objective of this study was to reduce the risk of errors when administering oral medications to infants aged 28 days to 2 years.The method of the preliminary risk analysis (PRA) was implemented by a multidisciplinary group in a hospital service o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9c33ccedb81bf33399197b9ef423699d
https://pubmed.ncbi.nlm.nih.gov/24630313
https://pubmed.ncbi.nlm.nih.gov/24630313
Publikováno v:
Journal of Biochemical Toxicology. 10:161-169
The effect of a light stable retinoid (CD 367) was studied on sea urchin embryos. CD 367 did not affect sperm-egg interaction. In a range of concentrations between 10 and 100 microM, CD 367 delayed the first and the second cleavages. When added after
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaa55265022b646cd15876ac21051b8d
https://doi.org/10.1002/jbt.2570100307
https://doi.org/10.1002/jbt.2570100307
Autor:
C. Delescluse, Roger Rahmani, D. Botta-Fridlund, Madeleine Pralavorio, G. de Sousa, Y. Letreut, N. Ledirac
Publikováno v:
Toxicology in Vitro
Toxicology in Vitro, Elsevier, 1997, pp.443-450
Toxicology in Vitro, Elsevier, 1997, pp.443-450
Hepatocytes and keratinocytes are among the most widely used cells in pharmaco-toxicology, but a limitation of these models is the provision of human tissues on a regular basis. The suitability of HepG2, HaCaT and HESV cell lines as an acceptable sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a99578965236b7ca4eab064a0747cd1
https://pubmed.ncbi.nlm.nih.gov/20654333
https://pubmed.ncbi.nlm.nih.gov/20654333
Autor:
Marie-Cecile Lenoir, C. Delescluse, W.R. Pilgrim, Bruno Bernard, Jean-Michel Bernardon, Braham Shroot, Bernard Martin, Jean Maignan, Bruno Charpentier, Uwe Reichert
Publikováno v:
Biochemical and Biophysical Research Communications. 186:977-983
The action of retinoids on gene regulation is mediated by three distinct nuclear retinoic acid receptor (RAR) subtypes called RAR alpha, beta and gamma. Since RAR gamma is predominantly expressed in adult skin, specific ligands for this subtype could
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7601f12fe2302b4e6b09a43f87992d1
https://doi.org/10.1016/0006-291x(92)90842-9
https://doi.org/10.1016/0006-291x(92)90842-9